Abstract

A human body hosts a relatively independent microbiome including five major regional biomes (i.e., airway, oral, gut, skin, and urogenital). Each of them may possess different regional characteristics with important implications to our health and diseases (i.e., so-termed microbiome associated diseases). Nevertheless, these regional microbiomes are connected with each other through diffusions and migrations. Here, we investigate the within-body (intra-individual) distribution feature of microbiome diversity via diversity area relationship (DAR) modeling, which, to the best of our knowledge, has not been systematically studied previously. We utilized the Hill numbers for measuring alpha and beta-diversities and built 1,200 within-body DAR models with to date the most comprehensive human microbiome datasets of 18 sites from the human microbiome project (HMP) cohort. We established the intra-DAR profile (z-q pattern: the diversity scaling parameter z of the power law (PL) at diversity order q = 0–3), intra-PDO (pair-wise diversity overlap) profile (g-q), and intra-MAD (maximal accrual diversity) profile (Dmax-q) for the within-body biogeography of the human microbiome. These profiles constitute the “maps” of the within-body biogeography, and offer important insights on the within-body distribution of the human microbiome. Furthermore, we investigated the heterogeneity among individuals in their biogeography parameters and found that there is not an “average Joe” that can represent majority of individuals in a cohort or population. For example, we found that most individuals in the HMP cohort have relatively lower maximal accrual diversity (MAD) or in the “long tail” of the so-termed power law distribution. In the meantime, there are a small number of individuals in the cohort who possess disproportionally higher MAD values. These findings may have important implications for personalized medicine of the human microbiome associated diseases in practice, besides their theoretical significance in microbiome research such as establishing the baseline for the conservation of human microbiome.

Highlights

  • The diversity-area relationship (DAR) (Ma, 2017) is a natural extension of the traditional species area relationship (SAR)

  • We investigate the within-body biogeography of the human microbiome by fitting two selected diversity area relationship (DAR) models (PL and power law with exponential cutoff (PLEC)) to each of the 150 individuals in the human microbiome project (HMP) cohort, for both alpha- and beta-diversity scaling respectively

  • The DAR models were constructed by accruing diversities across all the sites of an individual sampled in the HMP cohort

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Summary

Introduction

The diversity-area relationship (DAR) (Ma, 2017) is a natural extension of the traditional species area relationship (SAR). The later development of SAR in microbial world was because majority of bacteria in nature are still uncultivable and they are not detectable without resorting to the sequencing technology or other lesser powerful molecular marking technologies such as FISH and T-RFLP. It is the metagenomics technology, which can efficiently sequence the genomes of most species in a microbial community sample, that made it possible for the US NIH and European Union to launch the human microbiome project (HMP) and MetaHIT (Metagenomics of the Human Intestinal) respectively a decade ago (Turnbaugh et al, 2007; Human Microbiome Project, 2012a,b; Lozupone et al, 2012; http:// metahit.eu/). HMP and MetaHIT generated unprecedented opportunities and datasets to test some of the most important ecological theories and laws for the first time in the world of human microbiome, arguably the closest ecosystem to the humans

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